Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ulrich W. Gerwarth"'
Autor:
Werner Behrendt, Ulrich W. Gerwarth, Reinhard Haubold, Jörn v. Jouanne, Hannelore Keller-Rudeck, Dieter Koschel, Hans Schäfer, Joachim Wagner, Jörn Jouanne, Hannelore Keller-Rudek
This volume C 1 is the first supplement volume to'Phosphor'C which was published in 1965 and covers the compounds of phosphorus. Starting with the binary species formed between phosphorus and hydrogen, the present volume deals with the neutral mononu
Autor:
Joachim Wagner, Ulrich W. Gerwarth, Reinhard Haubold, Werner Behrendt, Hannelore Keller-Rudek, Dieter Koschel, Hans Schäfer, Jörn von Jouanne
Publikováno v:
P Phosphorus ISBN: 9783662088494
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35346eb6c0a5273bd67638363b15a2f9
https://doi.org/10.1007/978-3-662-08847-0_1
https://doi.org/10.1007/978-3-662-08847-0_1
Autor:
Werner Behrendt, Ulrich W. Gerwarth, Reinhard Haubold, Jörn v. Jouanne, Hannelore Keller-Rudek, Dieter Koschel, Hans Schäfer, Joachim Wagner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fea25f02c3231b36a31717434b4774e
https://doi.org/10.1007/978-3-662-08847-0
https://doi.org/10.1007/978-3-662-08847-0
Autor:
Ulrich W. Gerwarth
Publikováno v:
Die Makromolekulare Chemie. 181:1591-1604
2-Ethyl-1,3,2-dioxaboracycloalkanes polymerize more slowly than the analogous 2-aryl compounds. This is due to a difference in the bond type of the O—B—O group as shown by IR spectra and mass spectra. For the polymerization of 2-aryl-1,3,2-dioxab
Autor:
Ulrich W . Gerwarth
Publikováno v:
Zeitschrift für Naturforschung B. 34:1084-1091
The metathetic rearrangement of boron heterocycles containing an O - B (R) - O group with trivalent boron leads to oligomeric and/or polymeric ring systems. The equilibrium between the rings of different size is disturbed when crystallisation takes p
Autor:
Ulrich W . Gerwarth
Publikováno v:
Zeitschrift für Naturforschung B. 32:1408-1415
The condensation of phenyldihydroxyborane with pentane-1,5-diols yields no 1,3,2-dioxabora-cyclooctanes but oligomeric boron heterocycles. Their formation can be explained by an exchange of ligands of the boron atom, a process analogous to metathetic
Publikováno v:
Journal of Organometallic Chemistry. 145:1-16
During the aminoboration of appropriate double bond systems with 1,3,2-diazabora-cycloalkanes the heterocyclic ring system is expanded by insertion of two atoms of the double bond system. Collected data of comparative compounds enable us now to give